Organosilicon compounds, process for their production and their use

ABSTRACT

Abstract Organosilicon compounds having the formula I and/or II  
                 
 
     wherein R 1  is a mixture and the proportion of one component of the mixture is 10 to 50 mol %, are produced by reacting silanes having the formula III  
                 
 
     with mixtures of alcohols having the general formula R 1 —OH, with elimination of R—OH, and R—OH is continuously separated off from the reaction mixture by distillation. The organosilicon compounds can be used in rubber compounds.

INTRODUCTION AND BACKGROUND

[0001] The present invention concerns organosilicon compounds, a process for their production and their use.

[0002] The use of silanes as coupling agents is known. Thus aminoalkyl trialkoxysilanes, methacryloxyalkyl trialkoxysilanes, polysulfanalkyl trialkoxysilanes and mercaptoalkyl trialkoxysilanes are used as coupling agents between inorganic materials and organic polymers, as crosslinking agents and surface modifiers (E. P. Plueddemann, “Silane Coupling Agents”, 2^(nd) Ed. Plenum Press 1982).

[0003] These coupling agents or bonding agents form bonds to both the filler and the elastomer, thus creating a good interaction between the filler surface and the elastomer.

[0004] It is also known that the use of commercial silane coupling agents (DE 22 55 577) with three alkoxy substituents at the silicon atom leads to the release of considerable amounts of alcohol during and after bonding to the filler. Since trimethoxy- and triethoxy-substituted silanes are generally used, the corresponding alcohols, methanol and ethanol, are released in considerable quantities.

[0005] It is also known from DE 10015309 that the use of a mercaptosilane in combination with a long-chain alkyl silane leads to rubber compounds with increased reinforcement and reduced hysteresis loss. The alkyl silane is needed to ensure reliable processability of the rubber compound.

[0006] A disadvantage of the known mercaptosilanes according to DE 10015309 is the need to add alkyl silanes to rubber compounds in order to obtain particular properties.

[0007] It is also known that methoxy- and ethoxy-substituted silanes are more reactive than the corresponding long-chain alkoxy-substituted silanes and can therefore bond more quickly to the filler, such that from a technical and economic perspective the use of methoxy and ethoxy substituents cannot be avoided.

[0008] Organosilicon compounds having the general formula

[0009] are known from DE 10137809

[0010] wherein R is a methyl or ethyl group,

[0011] R′ is the same or different and a C₉-C₃₀ branched or unbranched monovalent alkyl or alkenyl group, aryl group, aralkyl group, branched or unbranched C₂-C₃₀ alkyl ether group, branched or unbranched C₂-C₃₀ alkyl polyether group,

[0012] R″ is a branched or unbranched, saturated or unsaturated, aliphatic, aromatic or mixed aliphatic/aromatic divalent C₁-C₃₀ hydrocarbon group,

[0013] X is NH_((3−n)) where n=1,2,3 and m=1, O(C═O)—R″′ where n=1 and m=1, SH where n=1 and m=1, S where n=2 and m=1-10 and mixtures thereof, S(C═O)—R″′ where n=1 and m=1 or H where n=1 and m=1,

[0014] where R″′ equals C₁-C₃₀ branched or unbranched alkyl or alkenyl group, aralkyl group or aryl group.

[0015] A disadvantage of the known organosilicon compounds according to DE 10137809 is the low hardness and dynamic rigidity in rubber compounds.

[0016] The object of the invention is to provide an organosilicon compound with which good hardness and dynamic rigidity values can be achieved in rubber compounds.

[0017] The object of the invention is also to provide an organosilicon compound with which comparable properties to those in DE 10015309 can be achieved in rubber compounds even without the addition of alkyl silanes.

SUMMARY OF THE INVENTION

[0018] The present invention provides organosilicon compounds having the formula I and/or II

[0019] wherein R is methyl or ethyl,

[0020] R¹ is the same or different and a C₉-C₃₀ branched or unbranched monovalent alkyl,

[0021] R² is a branched or unbranched, saturated or unsaturated, aliphatic, aromatic or mixed aliphatic/aromatic divalent C₁-C₃₀ hydrocarbon,

[0022] which are characterised in that R¹ is a mixture and the proportion of one component of the mixture is 10 to 50 mol %, preferably 10 to 40 mol %, particularly preferably 15 to 30 mol %.

[0023] R¹ can for example consist of 10 to 50 mol % C₁₄H₂₉ and 90 to 50 mol % C₁₂H₂₅ or of 10 to 50 mol % C₁₈H₃₇ and 90 to 50 mol % C₁₆H₃₃. R¹ can also consist of more than two different R¹ compounds.

[0024] R² can denote CH₂, CH₂CH₂, CH₂CH₂CH₂, CH₂CH₂CH₂CH₂, CH(CH₃), CH₂CH(CH₃), C(CH₃)₂, CH(C₂H₅), CH₂CH₂CH(CH₃), CH₂CH(CH₃)CH₂ or

[0025] The invention also provides a process for producing organosilicon compounds having the general formula I and/or II, which is characterised in that silanes having the general formula III

[0026] wherein R and R² have the meaning cited above, are reacted with mixtures of alcohols having the general formula R¹—OH, wherein R¹ has the meaning cited above and is used as a mixture of at least two alcohols (R¹ is different), with elimination of R—OH, and R—OH is continuously separated off from the reaction mixture by distillation.

[0027] Alcohol mixtures comprising 10 to 50 mol % C₁₄H₂₉OH and 90 to 50 mol % C₁₂H₂₅OH or alcohol mixtures comprising 10 to 50 mol % C₁₈H₃₇OH and 90 to 50 mol % C₁₆H₃₃OH can be used, for example. Alcohol mixtures comprising several components (R¹) can also be used. Lorol Spezial or Stenol 1618 (cetyl/stearyl alcohol) produced by Cognis or Ecorol 68/50 (cetyl stearyl alcohol) produced by Ecogreen Oleochemicals, for example, can be used as R¹—OH alcohol mixtures.

[0028] In the process according to the invention a mixture can be formed in which none, one, two or three of the RO groups are replaced by R¹O groups. The ratio of RO to R¹O groups can be determined by the molar ratio of the silane having the general formula III to the alcohol having the formula R¹—OH. For example, an organosilicon compound having an average analysis according to formula I can be obtained by reacting two molar equivalents of the alcohol mixture having the formula R¹—OH with one molar equivalent of the silane having the general formula III. For example, an organosilicon compound having an average analysis according to formula II can be produced by reacting one molar equivalent of the alcohol mixture having the general formula R¹—OH with one molar equivalent of the silane having the general formula III.

[0029] The reaction can be accelerated by means of neutral, acid or basic catalysts, such as e.g. hydrochloric acid, sulfuric acid, phosphoric acid, formic acid, acetic acid, toluene-para-sulfonic acid, sodium hydroxide solution, potassium hydroxide solution, sodium methylate, sodium ethylate, ion-exchange resins Amberlyst 15, Deloxan ASP I/9 or metal compounds, in particular titanates, known for example from U.S. Pat. No. 2,820,806.

[0030] The reaction can be performed at temperatures between 20 and 200° C., preferably between 20 and 150° C. In order to avoid condensation reactions it can be advantageous to perform the reaction in a moisture-free atmosphere, ideally in an inert gas atmosphere.

[0031] The organosilicon compounds according to the invention can be used as coupling agents between inorganic materials (for example glass fibres, metals, oxidic fillers, silicas) and organic polymers (for example thermosets, thennoplastics, elastomers), or as crosslinking agents and surface modifiers. The organosilicon compounds according to the invention can be used as coupling agents in tires made from rubber filled with silica and/or starch.

[0032] The invention also provides rubber compounds that are characterized in that they contain rubber, filler, such as e.g. precipitated silica, optionally other rubber auxiliary substances, and at least one organosilicon compound according to the invention.

[0033] The organosilicon compound according to the invention can be used in quantities of 0.1 to 20 wt. %, relative to the quantity of rubber used.

[0034] Addition of the organosilicon compounds according to the invention and addition of the fillers can preferably take place at material temperatures of 100 to 200° C. However, it can also take place later at lower temperatures (40 to 100° C.), for example together with other rubber auxiliary substances.

[0035] The organosilicon compound can be added to the mixing process both in pure form and attached to an inert organic or inorganic support. Preferred supporting materials are silicas, waxes, thermoplastics, natural or synthetic silicates, aluminum oxide or carbon blacks. The following fillers can be used as fillers for the rubber compounds according to the invention:

[0036] Carbon blacks: The carbon blacks to be used here are produced by the lamp black, furnace or channel black process and have BET surface areas of 20 to 200 m²/g, such as e.g. SAF, ISAF, HSAF, HAF, FEF or GPF carbon blacks. The carbon blacks can optionally also contain heteroatoms such as Si for example.

[0037] Highly disperse silicas, produced for example by precipitation of solutions of silicates or flame hydrolysis of silicon halides with specific surface areas of 5 to 1000, preferably 20 to 400 m²/g (BET surface area) and with primary particle sizes of 10 to 400 nm. The silicas can optionally also be present as mixed oxides with other metal oxides, such as Al, Mg, Ca, Ba, Zn and titanium oxides.

[0038] Synthetic silicates, such as aluminum silicate, alkaline-earth silicates such as magnesium silicate or calcium silicate, with BET surface areas of 20 to 400 m²/g and primary particle diameters of 10 to 400 nm.

[0039] Synthetic or natural aluminum oxides and hydroxides

[0040] Natural silicates, such as kaolin and other naturally occurring silicas.

[0041] Glass fibres and glass fibre products (mats, strands) or glass microbeads.

[0042] Highly disperse silicas, produced by precipitation of solutions of silicates, with BET surface areas of 20 to 400 m²/g, can preferably be used in quantities of 5 to 150 parts by weight, relative in each case to 100 parts of rubber.

[0043] The cited fillers can be used alone or in a mixture.

[0044] In a particularly preferred embodiment, 10 to 150 parts by weight of light-colored fillers, optionally together with 0 to 100 parts by weight of carbon black, and 1 to 10 parts by weight of the organosilicon compound according to the invention having formula I and/or II, relative in each case to 100 parts by weight of rubber, can be used to produce the compounds.

[0045] In addition to natural rubber, synthetic rubbers are also suitable to produce the rubber compounds according to the invention. Preferred synthetic rubbers are described for example in W. Hofmann, Kautschuktechnologie, Genter Verlag, Stuttgart 1980. They include inter alia

[0046] Polybutadiene (BR)

[0047] Polyisoprene (IR)

[0048] Styrene/butadiene copolymers with styrene contents of 1 to 60, preferably 2 to 50 wt. % (SBR)

[0049] Isobutylene/isoprene copolymers (IIR)

[0050] Butadiene/acrylonitrile copolymers with acrylonitrile contents of 5 to 60, preferably 10 to 50 wt. % (NBR)

[0051] Partially hydrogenated or wholly hydrogenated NBR rubber (HNBR)

[0052] Ethylene/propylene/diene copolymers (EPDM)

[0053] and mixtures of these rubbers. For the production of motor vehicle tires, anionically polymerized S-SBR rubbers (solution SBR) with a glass transition temperature above −50° C. and mixtures thereof with diene rubbers are of particular interest.

[0054] The rubber vulcanizates according to the invention can contain additional rubber auxiliary substances, such as reaction accelerators, antioxidants, heat stabilizers, light stabilizers, antiozonants, processing aids, plasticizers, tackifiers, blowing agents, dyes, pigments, waxes, extenders, organic acids, retarders, metal oxides and activators, such as triethanolamine, polyethylene glycol, hexanetriol, which are known to the rubber industry.

[0055] The rubber auxiliary substances can be used in known quantities, which are governed inter alia by the intended use. Conventional quantities are for example quantities of 0.1 to 50 wt. %, relative to rubber. Sulfur or sulfur-doning substances can be used as crosslinking agents. The rubber compounds according to the invention can moreover contain vulcanization accelerators. Examples of suitable principal accelerators are mercaptobenzothiazoles, sulfenamides, thiurams, dithiocarbamates, particularly preferably sulfenamides, in quantities of 0.5 to 3 wt. %. Examples of co-accelerators are guanidines, thioureas and thiocarbonates in quantities of 0.5 to 5 wt. %. Sulfur can conventionally be used in quantities of 0.1 to 10 wt. %, preferably 1 to 3 wt. %, relative to rubber.

[0056] Vulcanization of the rubber compounds according to the invention can take place at temperatures from 100 to 200° C., preferably 130 to 180° C., optionally under pressure of 10 to 200 bar. The rubbers can be mixed with the filler, optionally rubber auxiliary substances and the organosilicon compound according to the invention in known mixing units, such as rolls, internal mixers and compounding extruders.

[0057] The rubber compounds according to the invention are suitable for the production of moulded parts, for example for the production of pneumatic tires, tire treads, cable sheaths, hoses, drive belts, conveyor belts, roll coverings, tires, shoe soles, sealing rings and damping elements.

[0058] The organosilicon compounds according to the invention can be used together with large-surface-area silicas with CTAB 180-220 m²/g in rubber compounds, in particular in truck tire treads.

[0059] The rubber compound according to the invention can be used for the production of tire treads with improved, lower rolling resistance, improved wet skid resistance and equally good dry performance as compared with a similar rubber compound in which the organosilicon compound according to the invention is exchanged for bis-(3-triethoxysilylpropyl) tetrasulfide in a molar ratio relative to the silicon units of 1:1.8 to 1:2.7.

[0060] The rubber compound according to the invention can be used for the production of tire treads with improved, lower rolling resistance and improved wet skid resistance with equally good abrasion resistance as compared with a similar rubber compound in which the organosilicon compound according to the invention is exchanged for bis-(3-triethoxysilylpropyl) tetrasulfide in a molar ratio relative to the silicon units of 1:1.8 to 1:2.7.

[0061] The organosilicon compounds according to the invention have the advantage compared with organosilicon compounds according to DE 10137809 that hardness and dynamic rigidity E* are increased while tan δ 60° C. (correlated with rolling resistance) remains the same.

[0062] The organosilicon compounds according to the invention have the advantage that less methanol or ethanol is released than is the case with the known silanes while the reactivity remains the same. Due to their inactivity the non-volatile alcohols are not separated from the organosilicon compound or because of their non-volatility they remain in the polymer matrix. In both cases they are not released into the environment.

[0063] In addition, the organosilicon compounds according to the invention have the advantage that there is no need to add alkyl silane as described in DE 10015309, since in the organosilicon compounds according to the invention having formula I and/or II no deterioration in processability, as in the case of e.g. 3-mercaptopropyl trimethoxysilane or 3-mercaptopropyl triethoxysilane, has been found.

[0064] The rubber compounds according to the invention have the advantage as compared with rubber compounds containing bis-(3-triethoxysilylpropyl) tetrasulfide that dynamic rigidity is reduced and they are therefore especially suitable for winter tires (soft formulation).

BRIEF DESCRIPTION OF DRAWING

[0065]FIG. 1 is a representation of a driving test track. The dots in FIG. 1 are measuring points on x, y-coordinates of the test track. The measuring points are linked with straight lines.

DETAILED EMBODIMENT OF THE INVENTION EXAMPLES: Example 1:

[0066] A mixture consisting of 286.1 g 3-mercaptopropyl triethoxysilane (formula III where R=CH₂CH₃, R²=—CH₂CH₂CH₂—), 313.1 g dodecanol (R¹=—C₁₂H₂₅) and 154.4 g 1-tetradecanol (R¹ =—C₁₄H₂₉) is heated with 140 μl tetra-n-butyl orthotitanate to 110° C. in a 1-litre flask in a rotary evaporator and ethanol that is produced is distilled off over 4 h in vacuo at 40 mbar. 636.86 g (99.0%) of a colorless liquid having formula I, where R=—CH₂CH₃, R¹ =—C_(12.6)H_(26.2), R²=—CH₂CH₂CH₂—), is obtained.

Example 2

[0067] Production and analysis of the rubber compounds according to the invention The formulation used for the rubber compounds is set out in Table 1 below. The unit phr denotes contents by weight, relative to 100 parts of the crude rubber used. The organosilicon compound according to the invention is added in equimolar quantities to 3-mercaptopropyl triethoxysilane relative to silicon. The general process for the production of rubber compounds and vulcanizates thereof is described in the book: “Rubber Technology Handbook”, W. Hofmann, Hanser Verlag 1994. TABLE 1 Compound 1 Compound 2 Reference Reference Compound 3 Stage 1 Buna VSL 5025-1 96 96 96 Buna CB 24 30 30 30 Ultrasil 7000 GR 80 80 80 3-mercaptopropyl 2.4 — — triethoxysilane VP Si 208 2.5 — — Organosilicon compound — 5.7 — according to example 10 DE 10137809.2 Organosilicon compound — — 5.4 according to example 1 ZnO 2 2 2 Stearic acid 2 2 2 Naftolen 10 10 10 Vulkanox 4020 1.5 1.5 1.5 Protektor G35P 1 1 1 Stage 2 Batch from stage 1 Stage 3 Batch from stage 2 Vulkacit D 2 2 2 Vulkazit CZ 1.5 1.5 1.5 TBzTD 0.2 0.2 0.2 Sulfur 2.3 2.3 2.3

[0068] The polymer VSL 5025-1 is a solution-polymerized SBR copolymer from Bayer AG with a styrene content of 25 wt. % and a butadiene content of 75 wt. %. The copolymer contains 37.5 phr oil and displays a Mooney viscosity (ML 1+4/100° C.) of 50±4.

[0069] The polymer Buna CB 24 is a cis-1,4-polybutadiene (neodymium type) from Bayer AG with a cis-1,4 content of at least 97% and a Mooney viscosity of 44±5.

[0070] Naftolen ZD from Chemetall is used as aromatic oil. Vulkanox 4020 is a 6PPD from Bayer AG and Protektor G35P is an antiozonant wax from HB-Fuller GmbH. Vulkacit D (DPG) and Vulkazit CZ (CBS) are commercial products from Bayer AG.

[0071] Ultrasil 7000 GR is a readily dispersible precipitated silica from Degussa AG with a BET surface area of 170 m²/g. 3-mercaptopropyl triethoxysilane is produced by ABCR GmbH CoKG and VP Si 208, octyl triethoxysilane, is a commercial product from Degussa AG.

[0072] The rubber compounds are produced in an internal mixer in accordance with the mixing instructions in Table 2. TABLE 2 Stage 1 Settings Mixing unit Werner & Pfleiderer E-type Speed 70 rpm Ram force 5.5 bar Void volume 1.58 I Fill ratio 0.56 Flow temp. 80° C. Mixing process 0 to 1 min Buna VSL 5025-1 + Buna CB 24 1 to 3 min 1/2 filler, ZnO, stearic acid, Naftolen ZD, organosilicon compounds 3 to 4 min 1/2 filler, antioxidant 4 min Clean 4 to 5 min Mix, 5 min Clean 5 to 6 min Mix and remove Batch temp. 145-150° C. Storage 24 h at room temperature Stage 2 Settings Mixing unit As for stage 1 apart from: Speed 80 rpm Fill ratio 0.53 Mixing process 0 to 2 min Break up batch from stage 1 2 to 5 min Maintain batch temperature at 140-150° C. by varying speed 5 min Remove Batch temp. 150° C. Storage 4 h at room temperature Stage 3 Settings Mixing unit As for stage 1 except for Speed 40 rpm Fill ratio 0.51 Flow temp. 50° C. Mixing process 0 to 2 min Batch from stage 2, accelerator, sulfur 2 min Remove and sheet out on laboratory mixing rolls, (diameter 200 mm, length 450 mm, flow temperature 50° C.) Homogenize: Score 3× on left, 3× on right and fold over and pass through 8× with narrow nip (1 mm) and 3× with wide nip (3.5 mm) Remove sheet Batch temp. 85-95° C.

[0073] The rubber test methods are set out in Table 3. TABLE 3 Physical test Standard/conditions ML 1 + 4, 100° C., stage 3 DIN 53523/3, ISO 667 Cure-meter test, 165° C. DIN 53529/3, ISO6502 t10% and t90% (min) Tensile test on ring, 23° C. DIN 53504, ISO 37 Tensile strength (MPa) Moduli (MPa) Elongation at break (%) Shore-A hardness, 23° C. (SH) DIN 53 505 Viscoelastic properties, DIN 53 513, ISO2856 0 and 60° C., 16 Hz, 50 N initial force and 25 N amplitude force Dynamic modulus E* (MPa) Loss factor tan δ () Ball rebound, 60° C. (%) ASTM D 5308 Goodrich flexometer DIN 53 533, 0.25 inch stroke, 25 min, 23° C. ASTM D 623 A Contact temperature (° C.) Center temperature (° C.) Permanent set (%) DIN abrasion, 10 N force (mm³) DIN 53 516

[0074] Table 4 shows the results from the rubber tests. The compounds are vulcanized for 20 min at 165° C. TABLE 4 Features Unit 1 2 3 Results for unvulcanized mix ML(1 + 4) at 100° C/, stage 3 [MU] 69 62 72 MDR, 165° C., 0,5° t 10% [min] 0.8 1.0 0.8 t 90% [min] 5.9 15.6 16.8 Results for vulcanizate Tensile test on ring Modulus 100% [MPa] 2.1 2.1 2.4 Modulus 200% [MPa] 6.7 7.1 7.5 Modulus 300% [MPa] 13.8 — — Modulus 300%/100% [—] 6.6 — — Tensile strength [MPa] 14.1 12.7 13.2 Elongation at break [%] 300 270 280 Shore-A hardness [SH] 58 55 61 Ball rebound 60° C. [%] 69.0 70.2 69.7 DIN abrasion [mm³] 62 34 50 Goodrich flexometer Contact temperature [° C.] 49 52 52 Centre temperature [° C.] 87 91 90 Permanent set [%] 1.5 1.3 1.7 MTS Dynamic modulus E*, 0° C. [MPa] 12.2 10.0 12.3 Dynamic modulus E*, 60° C. [MPa] 6.3 5.9 6.8 Loss factor tan δ, 0° C. [—] 0.471 0.413 0.428 Loss factor tan δ, 60° C. [—] 0.086 0.083 0.084

[0075] As can be seen from Table 4, compound 3 with the organosilicon compound according to the invention displays good hydrophobing and reinforcement. In particular, the moduli and Shore-A hardness for compound 3 according to the invention are higher than those for the reference compounds. In addition, the dynamic rigidity (dynamic modulus E*) of compound 3 according to the invention is higher than that of reference compound 2, with almost the same loss factor tan δ 60° C. Even without the addition of alkyl silane, compound 3 displays virtually the same dynamic rigidity and tanδ 60° C. values as compound 1 with alkyl silane.

Example 3

[0076] 268.08 g 3-mercaptopropyl triethoxysilane and a mixture consisting of 313.05 g 1-dodecanol and 154.36 g 1 tetradecanol are placed in a 1-litre three-necked flask with distillation attachment at room temperature and 1.0 g toluene-p-sulfonic acid monohydrate is added. The solution is heated to 120° C. The ethanol that is produced is continuously removed by distillation. Distillation is then performed in a rotary evaporator in vacuo at 80° C. and 20 mbar. 638.7 g (99%) of a colorless liquid according to formula I is obtained, where R=—CH₂CH₃, R¹=mixture of —C₁₂H₂₅ and —C₁₄H₂₉ in the ratio 2:1 and R²=—CH₂CH₂CH_(2—.)

Example 4

[0077] Production and Analysis of the Rubber Compounds According To The Invention

[0078] The formulation used for the rubber compounds is set out in Table 5 below. The silane according to the invention is added in equimolar quantities to Si 69, relative to silicon. The sulfur adjustment is necessary to compensate for the low sulfur content in the organosilicon compound according to the invention. TABLE 5 A B Basic compound Rubber blend ¹⁾: S-SBR/BR/NR 100 100 Highly dispersible silica ²⁾ 80 80 Carbon black ³⁾ 6.6 6.6 Aromatic plasticizer 30 24 Si 69 ⁴⁾ 6.6 — Organosilicon compound according to example 3 — 5.95 Chemicals ⁵⁾ Ready-to-use compound Ground sulfur 2.0 2.8 Accelerator mixture ⁶⁾

[0079] The rubber compounds are produced in an internal mixer in a four-stage process. All components of the basic compound are mixed in the first mixing stage, followed by two intermediate stages and a final stage in which the accelerators and the sulfur are added. The mixing temperatures in the first three mixing stages range from 140 to 160° C. and the temperature in the fourth stage is <120° C.

[0080] The rubber test methods are set out in Table 6. TABLE 6 Physical test Standard/conditions ML 1 + 4, 100° C. stage 3 DIN 53523/3, ISO 667 Cure-meter test, 165° C. DIN 53529/3, ISO 6502 Dmax-Dmin (dNm) t10% and t90% (min) Tensile test on ring, 23° C. DIN 53504, ISO 37 Tensile strength (MPa) Moduli (MPa) RF (modulus 300%/modulus 100%) Elongation at break (%) Shore-A hardness, 23° C. (SH) DIN 53 505 Viscoelastic properties, DIN 53 513, ISO 2856 0 and 60° C., 16 Hz, 50 N initial force and 25 N amplitude force Dynamic modulus E* (MPa) Loss factor tan δ () Goodrich flexometer 0.25 inch stroke, 25 min, 23° C. DIN 53 533, ASTM D 623 centre temperature (° C.) DIN abrasion, 10 N force (mm³) DIN 53 516

[0081] Table 7 shows the results from the rubber tests. The compounds are vulcanized for 10 min at 165° C. TABLE 7 Unit A B Data for unvulcanized mix ML (1 + 4) [—] 50 49 Dmax-Dmin [dNm] 20.5 15.2 t10% [min] 2.0 1.1 t90% [min] 5.1 3.8 Data for vulcanizate Tensile strength [MPa] 13.5 12.6 Modulus 100% [MPa] 2.8 2.0 Modulus 300% [MPa] 10.0 9.5 RF [—] 3.6 4.8 Elongation at break [%] 390 370 Shore-A hardness [—] 74 63 E* (60° C.) [MPa] 9.2 7.8 tan δ (60° C.) [—] 0.142 0.111 tan δ (0° C.) [—] 0.392 0.346 Center temperature [° C.] 134 122 DIN abrasion [mm³] 59 49

[0082] As can be seen from the data in Table 7, the Mooney viscosity of compound B according to the invention is at the same level as reference compound A. Compound B is characterized in particular by a low dynamic rigidity (E*), a high reinforcement factor (RF) with reduced DIN abrasion and a reduced hysteresis loss (tan δ, center temperature).

[0083] The two tire tread compounds A and B are used to build test tires A and B of size 205/65R15 94V, and these are tested by Smithers Scientific Services Inc. Table 8 reproduces the test types and test conditions used. The road tests are performed with a BMW 528i. The front tire pressure is 2.1 bar, the rear tire pressure 2.5 bar. The front load is 903 kg, the rear 911 kg. The relative rating of test tire B with compound B according to the invention relative to reference tire A is shown in Table 9. Values over 100 indicate an improvement. TABLE 8 Rolling resistance ASTM J-1269; 572 kg , 2.0 bar ABS wet braking Stopping distance from 80 km/h ABS dry braking Stopping distance from 80 km/h Wet handling Circuit time for curve section (FIG. 1) Dry handling Circuit time for curve section (FIG. 1)

[0084]FIG. 1 illustrates the curve section of the test track. TABLE 9 Test tire B Rolling resistance 105 ABS wet braking 103 ABS dry braking 100 Wet handling  99 Dry handling  99

[0085] As can be seen, the tire rolling resistance and ABS wet braking are significantly improved. Within the framework of conventional fluctuations, the handling performance is similar. The DIN abrasion value in Table 7 indicates an improved abrasion value.

[0086] Further variations and modifications will be apparent from the foregoing to those skilled in the art and are intended to be encompassed by the claims appended hereto.

[0087] German priority application 102 23 658.5 filed May 28, 2002 is relied on and incorporated herein by reference. 

We claim:
 1. An organosilicon compound having the formula I or II

wherein R is a methyl or ethyl, R¹ is the same or different and is a C₉-C₃₀ branched or unbranched monovalent alkyl, R² is a branched or unbranched, saturated or unsaturated, aliphatic, aromatic or mixed aliphatic/aromatic divalent C₁-C₃₀ hydrocarbon, and R¹ is a mixture and the proportion of one component of the mixture is 10 to 50 mol %.
 2. The organosilicon compound according to claim 1, wherein the proportion of one component of the mixture is 10 to 40 mol %.
 3. The organosilicon compound according to claim 1, wherein the proportion of one component of the mixture is 15 to 30 mol %.
 4. The organosilicon compound according to claim 1, wherein R² denotes a member selected from the group consisting of CH₂, CH₂CH₂, CH₂CH₂CH₂, CH₂CH₂CH₂CH₂, CH(CH₃), CH₂CH(CH₃), C(CH₃)₂, CH(C₂H₅), CH₂CH₂CH(CH₃), CH₂CH(CH₃)CH₂ and


5. A process for the production of an organosilicon compound according to claim 1, comprising reacting a silane having the formula III

wherein R is methyl or ethyl and R² is a branched or unbranched, saturated or unsaturated, aliphatic, aromatic or mixed aliphatic/aromatic divalent C₁C₃₀ hydrocarbon, with mixtures of alcohols having the general formula R¹—OH, to form a reaction mixture, wherein R¹ is different and is a C₉ C₃₀ branched or unbranched monovalent alkyl, to form R—)H, and continuously separating off R—OH from the reaction mixture by distillation.
 6. A rubber composition comprising a natural or synthetic rubber and an organosilicon compound according to claim
 1. 7. An organic polymer composition comprising an organic polymer and an organosilicon compound according to claim
 1. 8. Rubber compounds characterised in that they contain rubber, filler, optionally other rubber auxiliary substances and at least one organosilicon compound according to claim
 1. 9. A moulded part comprising natural or synthetic rubber or an organic polymer and an organosilicon compound according to claim
 1. 10. The moulded part according to claim 9 which is a pneumatic tire, tire tread, cable sheath, hose, drive belt, conveyor belt, roll covering, tire, shoe sole, sealing ring or a damping element.
 11. A tire tread comprising rubber in which the organosilicon compound according to claim 1 is exchanged for bis-(3-triethoxysilylpropyl) tetrasulfide in a molar ratio relative to the silicon units of 1:1.8 to 1:2.7.
 12. A rubber compound for the production of tire treads in which the organosilicon compound according to claim 1 is exchanged for bis-(3-triethoxysilylpropyl) tetrasulfide in a molar ratio relative to the silicon units of 1:1.8 to 1:2.7. 